The PROPEL study compared the safety and efficacy of ADYNOVATE®
[Antihemophilic Factor [Recombinant], PEGylated] following
pharmacokinetic (PK)-guided prophylaxis, targeting two different
factor VIII trough levels
The novel design of the study was built upon preliminary data
indicating that FVIII exposure associated with higher trough levels
may be able to help enhance bleed protection and help more patients
reach zero bleeds
Takeda’s strong inaugural presence at EAHAD underscores its
commitment to the hemophilia community following recent completion of
CAMBRIDGE, Mass. & OSAKA, Japan–(BUSINESS WIRE)–Takeda Pharmaceutical Company Limited (TSE:4502/NYSE:TAK)
(“Takeda”), the global biotechnology leader in rare diseases, has today
announced results from its phase IIIb/IV clinical trial for ADYNOVATE at
the 12th Annual Congress of the European Association of
Haemophilia and Allied Disorders (EAHAD), taking place 6-9
February, in Prague, Czech Republic. The PROPEL study is a PROspective,
randomized, multi-center study comparing the safety and efficacy of
ADYNOVATE following PK-guided prophylaxis targeting
two different Factor Eight (FVIII) trough Levels
in subjects with severe hemophilia A.
The study showed that ADYNOVATE prophylaxis targeting 8–12% (HIGH) vs
1–3 % (LOW) trough levels was associated with a trend toward a higher
proportion of patients with a total annualized all bleed rate (ABR)=0
(66% HIGH vs 39% LOW; p=0.075). The HIGH group was also associated with
a trend toward a lower total ABR, as well as a higher proportion of
patients with all annualized joint bleed rate (AJBR)=0 (90% HIGH vs 68%
LOW) and all spontaneous ABR=0 (84% HIGH vs 61% LOW). The data suggests
that optimizing FVIII profiles through PK-driven dosing that targets
trough levels 8-12% was consistently achievable and further treatment
personalization for patients with hemophilia A should be considered.
Safety profiles were comparable and consistent with previous ADYNOVATE
trials. Ongoing analyses will characterize the relationship between
PK-tailored dosing of ADYNOVATE FVIII levels and bleeding events.
“The study reiterates the importance of personalized prophylaxis for
those living with hemophilia,” said Dr. med. Robert Klamroth, Head of
the Department of Internal Medicine Angiology and Coagulation Disorders
and Director of the Comprehensive Care Haemophilia Treatment Center and
the Haemostasis and Thrombosis Unit at the Vivantes Klinikum in Berlin,
Germany. “The findings suggest the need to measure actual FVIII levels
and show a clear trend that if we’re able to keep FVIII levels in a
higher range, there may be better patient outcomes, including enhanced
bleed protection that could help more patients reach zero bleeds.”
“At Takeda, we are proud of the hematology heritage Shire and Baxalta
built over 60 years and we plan on expanding on it through continued
research and innovation, including continued focus on direct factor
replacement,” said Dr. med. Wolfhard Erdlenbruch, Vice President Head of
Global Medical Affairs Hematology, Takeda. “We are excited to be at
EAHAD and share the results of PROPEL study. The zero all bleed rates
and zero all spontaneous joint bleeds in this study have not been
reported previously with people living with hemophilia A. This supports
that factor levels matter and brings us a step closer to achieving our
goal of optimized and personalized patient care, because every bleed
In addition to PROPEL, Takeda will present a dozen scientific data
releases on the company’s recently acquired broad portfolio of
treatments for bleeding disorders throughout EAHAD, including:
AHEAD international and German studies: Effectiveness, safety, and
quality of life outcomes in hemophilia A patients treated with
antihemophilic factor (recombinant) in a real world setting over 5
Insights into the evolution of haemophiliac arthropathy: The Irish
personalised approach to the treatment of haemophilia (iPATH) study.
Physical activity and haemophilic joint arthropathy amongst adults
with severe haemophilia in Ireland: The Irish personalised approach to
the treatment of haemophilia (iPATH) study.
Barriers to physical activity amongst adults with moderate and severe
haemophilia in Ireland: The Irish personalised approach to the
treatment of haemophilia (iPATH) study.
Results from a phase 3B, open-label, multicenter, continuation study
of rurioctocog alfa pegol for prophylaxis in previously treated
patients with severe hemophilia A: Analysis by age group.
Design of a phase 3, prospective, multicenter, open-label study of
safety and hemostatic efficacy of rurioctocog alfa pegol in previously
untreated patients <6 years of age with severe hemophilia A.
Demographic and baseline data from patients with hemophilia and
inhibitors enrolled in the FEIBA global outcomes (“FEIBA GO”) study.
Analysis of joint bleeding events from a phase 3, multicenter,
open-label study of on-demand recombinant von Willebrand factor (VWF)
treatment in patients with severe von Willebrand disease (VWD).
Evaluation of laboratory safety data from patients with severe von
Willebrand disease (VWD) in association with infusion of recombinant
von Willebrand factor (VWF) in a phase 3, multicenter, open-label
Efficacy and safety of prophylaxis with recombinant von Willebrand
factor (VWF) in severe von Willebrand disease (VWD): Design of a
prospective, phase 3, open-label, international multicenter study.
Nonclinical safety evaluation of a next generation factor IX (FIX)
gene therapy construct (SHP648) in mice.
About the PROPEL Study
The PROPEL study evaluated the safety and efficacy of ADYNOVATE in
PK-guided prophylaxis targeting two different FVIII trough levels in
previously treated patients.
Methods: Eligible subjects had FVIII activity <1%, annualized
bleed rate (ABR) ≥2, and transitioned from a previous SHP660 (ADYNOVATE)
study or were 12–65 years old with ≥150 exposure days to plasma-derived
or recombinant FVIII. After initial PK assessments, subjects received 12
months of PK-guided prophylaxis targeting FVIII trough levels of 1–3%
(LOW) or 8–12% (HIGH) (1st 6 months: dose adjustment period).
Primary outcome was the % of subjects with a total ABR=0 (all bleeds)
during the 2nd 6-month study period. Secondary outcomes
included total ABR, spontaneous ABR and joint ABR (AJBR) (all bleeds),
and adverse events (AEs).
Results: Overall, 115 male subjects (57 LOW, 58 HIGH) received ≥1
SHP660 dose. Median (range) age was 28 (12–61) years; 106 subjects (56
LOW, 50 HIGH) completed the study. During the 2nd 6 months,
total ABR=0 was achieved by 22/57 (39%) LOW, 38/58 (66%; P=0.075) HIGH,
spontaneous ABR=0 by 35/57 (61%) and 49/58 (84%; P=0.141), respectively,
and AJBR=0 by 39/57 (68%) and 52/58 (90%; P=0.179). Mean (SD), median
(IQR) total ABRs for the 2nd 6-month period: 3.6 (7.3), 2.0
(4.0) LOW; 1.6 (3.3), 0 (2.0) HIGH. Overall AEs and SAEs occurred in 63%
and 9% of subjects, with 1 HIGH subject (0.9%) SAE considered related to
SHP660: a transient 0.6 BU inhibitor without evidence of anti-FVIII
binding, which resolved by study end. AE profiles were comparable and
consistent with previous SHP660 trials.
ADYNOVATE [Antihemophilic Factor (Recombinant),
PEGylated] was first approved by the Food and Drug Administration (FDA)
in the U.S. followed by approval in Japan, Canada, and Colombia, and is
approved as ADYNOVI® in the 28 Member States of the European Union (EU)
as well as Iceland, Liechtenstein, Norway and Switzerland. In Europe
ADYNOVI is approved for the treatment and prophylaxis of bleeding in
patients 12 years and above with hemophilia A.
ADYNOVI SAFETY INFORMATION FOR EUROPE
Please consult the ADYNOVI Summary of Product Characteristics (SmPC)
before prescribing, particularly in relation to dosing and treatment
Hypersensitivity to the active substance, to the parent molecule octocog
alfa or to any of the excipients listed in the SmPC. Known allergic
reaction to mouse or hamster protein.
Special warnings and precautions for use
The medicinal product contains traces of mouse and hamster proteins. If
symptoms of hypersensitivity occur, patients should be advised to
discontinue use of the medicinal product immediately and contact their
physician. Patients should be informed of the early signs of
hypersensitivity reactions including hives, generalised urticaria,
tightness of the chest, wheezing, hypotension, and anaphylaxis.
The formation of neutralising antibodies (inhibitors) against factor
VIII is a known complication in the management of individuals with
haemophilia A. These inhibitors are usually IgG immunoglobulins directed
against the factor VIII procoagulant activity, which are quantified in
Bethesda Units (BU) per ml of plasma using the modified assay.
In general, all patients treated with coagulation factor VIII should be
carefully monitored for the development of inhibitors by appropriate
clinical observations and laboratory tests. If the expected factor VIII
activity plasma levels are not attained, or if bleeding is not
controlled with an appropriate dose, testing for factor VIII inhibitor
presence should be performed.
After reconstitution this medicinal product contains 0.45 mmol sodium
(10 mg) per vial.
|Common (Greater-than or equal to 1/100 to <1/10)||Headache, Diarrhea, Nausea, Rash|
|Uncommon (Greater-than or equal to 1/1000 to <1/100)||
Factor VIII inhibition in previously-treated patients (PTPs),
For more information, please refer to the ADYNOVI Summary of Product
About Takeda Hematology
Following its recent acquisition of Shire, Takeda is a leader in
hemophilia with the longest heritage and market-leading portfolio,
backed by established safety and efficacy profiles with decades of real
We have 60+ years driving innovation for patients and a broad portfolio
of 11 products across 9 hemophilia indications. Our experience as
leaders in hematology means we are well prepared to meet today’s needs
as we pursue future developments in the care of bleeding
disorders. Together with the hematology community, we are raising
expectations for the future, including earlier diagnosis, earlier and
full protection against bleeds, and more personalized patient care.
About Takeda Pharmaceutical Company Limited
Takeda Pharmaceutical Company Limited (TSE:4502/NYSE:TAK)
is a global, values-based, R&D-driven biopharmaceutical leader
headquartered in Japan, committed to bringing Better Health and a
Brighter Future to patients by translating science into
highly-innovative medicines. Takeda focuses its R&D efforts on four
therapeutic areas: Oncology, Gastroenterology (GI), Neuroscience, and
Rare Diseases. We also make targeted R&D investments in Plasma-Derived
Therapies and Vaccines. We are focusing on developing highly innovative
medicines that contribute to making a difference in people’s lives by
advancing the frontier of new treatment options and leveraging our
enhanced collaborative R&D engine and capabilities to create a robust,
modality-diverse pipeline. Our employees are committed to improving
quality of life for patients and to working with our partners in health
care in approximately 80 countries and regions.
For more information, visit https://www.takeda.com
Media outside Japan